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JPS6236669B2 - - Google Patents
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JPS6236669B2 - - Google Patents

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Publication number
JPS6236669B2
JPS6236669B2 JP55110294A JP11029480A JPS6236669B2 JP S6236669 B2 JPS6236669 B2 JP S6236669B2 JP 55110294 A JP55110294 A JP 55110294A JP 11029480 A JP11029480 A JP 11029480A JP S6236669 B2 JPS6236669 B2 JP S6236669B2
Authority
JP
Japan
Prior art keywords
acetic acid
moromi
fermentation
concentration
acid concentration
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired
Application number
JP55110294A
Other languages
Japanese (ja)
Other versions
JPS5736976A (en
Inventor
Yoshio Kunimatsu
Koki Yamada
Shoji Oomori
Mikio Yamada
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
NAKANO SUTEN KK
Original Assignee
NAKANO SUTEN KK
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by NAKANO SUTEN KK filed Critical NAKANO SUTEN KK
Priority to JP11029480A priority Critical patent/JPS5736976A/en
Publication of JPS5736976A publication Critical patent/JPS5736976A/en
Publication of JPS6236669B2 publication Critical patent/JPS6236669B2/ja
Granted legal-status Critical Current

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  • Distillation Of Fermentation Liquor, Processing Of Alcohols, Vinegar And Beer (AREA)

Description

【発明の詳細な説明】[Detailed description of the invention]

本発明は食酢の製造法、特に通気発酵法による
半連続発酵で20%以上の高い酢酸濃度の食酢を製
造する方法に関するものである。 なお、本発明では特に断わらない限り、酢酸濃
度は重量/容量、アルコール濃度は容量/容量で
表わされるものとする。 従来、通気発酵法によつて高い酢酸濃度の食酢
を得るために様々な工夫がなされている。例えば
特開昭52−15899号の方法では、アルコールの添
加に関し工夫した半連続発酵法で高い酢酸濃度の
食酢を得たり、特開昭52−79092号、特開昭53−
41495号、特開昭53−44696号の方法などでは、増
殖槽と生酸槽をわけることで解決を試みている。 しかしながら、半連続発酵法では、次回の発酵
のために醪の一部を種酢とするので、自ずと酢酸
濃度に限界を生じ、また一方、増殖槽と生酸槽に
わけて酢酸菌の能力一杯まで生酸槽において高い
酢酸濃度まで発酵させるにしても、酢酸発酵にお
いては酢酸濃度が高くなればなる程、酢酸菌に対
して主生産物である酢酸の阻害が起るため、この
方法でも自ずと限界を生じ、いまだ20%以上の高
い酢酸濃度を有する食酢を通気発酵法で経済的に
製造した例はなく、この点でまだ改善すべき点を
残している。 本発明はこれら従来法の欠点を克服し、20%以
上という高い酢酸濃度を有する食酢を、通気発酵
法で半連続発酵を行なうことにより、効率良く製
造することを目的とするものであつて、本発明は
通気発酵タンクにアルコール、水、酢酸発酵液あ
るいは酢酸、及び酢酸菌の栄養物を用いて調製し
た醪を充填し、酢酸濃度15%以上で馴養した酢酸
菌を接種して通気下に発酵を開始させ、その後発
酵が進行し醪の酢酸濃度が充分上りアルコール濃
度が0.7〜2%となつたところで通気を中断する
ことなく醪の一部を残して他は取り出し、次に原
料醪を再充填して発酵を継続させ、以下同様にし
て醪の一部を取り出し、次に原料醪を再充填する
というようにしてサイクルを繰り返す半連続発酵
法での連続するサイクルにおいて、醪の酢酸濃度
が12〜15%となるまでは醪の温度を27〜32℃と
し、その後18℃を下限として醪の温度を27℃より
低い温度に低下させ20%以上の目的とする酢酸濃
度及びアルコール濃度が0.7〜2%となつたとこ
ろで通気を中断することなく醪の一部を残して他
は取り出し、次に原料醪を再充填して前回のサイ
クルと同様にして発酵を継続させ、さらに同様の
サイクルを繰り返すことによる通気発酵法で半連
続発酵を行なうことにより、20%以上の高い酢酸
濃度を有する酢酸発酵液を得ることを特徴とする
食酢の製造法である。 以下本発明について詳細に説明する。 従来より通気発酵法によつて食酢を製造する場
合、方法こそ種々異なるものの、その発酵温度範
囲としては発酵全期間を通じて26〜40℃、通常28
〜32℃の温度が採用されてきた。これは通気発酵
法による食酢の製造においては最適な温度条件と
して設定されたものであり、酢酸菌に対して環境
の変化を少なくするためにも重要とされてきた。 しかしながら、本発明者等は通気下の酢酸発酵
においては、用いられる酢酸菌は生酸と共に増殖
していく期間(以下、増殖期という)と、増殖は
停止し生酸のみを続ける期間(以下、生酸期とい
う)とに大別することができ、この2つの期間を
通じて温度を同じにすることこそが従来高い酢酸
濃度に達するのが困難であつた最大の原因と考え
た。すなわち、本発明者等は、この酢酸菌の特性
に注目して種々検討した結果、先に増殖期と生酸
期においてはその最適温度が異なることを見出
し、これに基いて、増殖期においては、醪の温度
を従来より知られて27〜32℃とし、その後、すな
わち生酸期においては醪の温度を増殖期の温度よ
り低温すなわち18〜24℃にする食酢の製造法(特
願昭54−14216号(特公昭56−21389号公報))、生
酸期において醪の温度を低下させる場合に、酢酸
濃度の増加に応じて醪の温度を2℃を越えない範
囲で低下させる食酢の製造法(特願昭54−129891
号(特開昭56−55193号公報))、及び生酸期にお
いて醪の温度を低下させる通気発酵と通気発酵に
よる半連続発酵法とを組み合わせた食酢の製造法
(特願昭54−136373号(特開昭56−61987号公
報))を発明した。 その後、さらに発酵に用いる酢酸菌、半連続発
酵法のサイクルでの醪の取り出し時におけるアル
コール濃度、及び醪の温度設定について種々研究
を続けた結果、ついに通気発酵による半連続発酵
法で20%以上の高い酢酸濃度を有する酢酸発酵液
を得ることのできる本発明に至つたのである。 そこでまず、発酵に用いる酢酸菌について検討
した結果を実験例を示して説明する。 実験例 1 通気発酵槽にアルコール、水、酢酸発酵液、及
び酢酸菌の栄養物を用いて調製した醪を再填し、
槽内の温度が30℃となつたところで酢酸菌を接種
して通気下に発酵を開始し、その後温調計により
醪の温度を約30℃に制御した。その時の酢酸濃度
は6.5%、アルコール濃度は3.5%であつた。 そして発酵が進み酢酸濃度が8.8%となつたと
ころでアルコール濃度が約50%のアルコールの添
加を開始した。さらに発酵が進み酢酸濃度が約13
%となつたところで温調計の設定を変更して26℃
とし、以後、酢酸濃度が約15%、約17%、約19%
の時に温調計の設定をそれぞれ24℃、22℃、20℃
とし、酢酸濃度が20.5%となつたところで醪の一
部を残して他は取り出し、原料醪を再充填して次
のサイクルの発酵を開始し、前のサイクルと同様
に発酵を継続させた。 この場合、酢酸菌として次の様な発酵を行なつ
ている発酵槽の酢酸菌を用い、これが発酵に及ぼ
す影響を調べた。その結果を示すと第1表のとお
りである。 A区分:酢酸濃度6%で連続発酵を行なつている
酢酸菌 B区分:酢酸濃度12〜13%で半連続発酵を行なつ
ている酢酸菌 C区分:酢酸濃度15〜16%で半連続発酵を行なつ
ている酢酸菌 D区分:酢酸濃度12〜13%で半連続発酵を行なつ
ているうち、時々15〜16%で醪の取り出しを行
なうサイクルを行なつている酢酸菌
The present invention relates to a method for producing vinegar, particularly a method for producing vinegar with a high acetic acid concentration of 20% or more by semi-continuous fermentation using an aerated fermentation method. In the present invention, unless otherwise specified, the acetic acid concentration is expressed in weight/volume, and the alcohol concentration is expressed in volume/volume. Conventionally, various efforts have been made to obtain vinegar with a high acetic acid concentration by the aerated fermentation method. For example, in the method of JP-A No. 52-15899, vinegar with a high acetic acid concentration is obtained by a semi-continuous fermentation method devised regarding the addition of alcohol;
Methods such as No. 41495 and JP-A-53-44696 attempt to solve this problem by separating the growth tank and the bioacid tank. However, in the semi-continuous fermentation method, a portion of the moromi is used as seed vinegar for the next fermentation, which naturally limits the acetic acid concentration. Even if fermentation is carried out to a high acetic acid concentration in a raw acid tank, the higher the acetic acid concentration in acetic acid fermentation, the more inhibited acetic acid, which is the main product, will occur for acetic acid bacteria. However, there is still no example of producing vinegar with a high acetic acid concentration of 20% or more economically using the aerated fermentation method, and in this respect, there is still room for improvement. The purpose of the present invention is to overcome the drawbacks of these conventional methods and efficiently produce table vinegar having a high acetic acid concentration of 20% or more by performing semi-continuous fermentation using an aerated fermentation method. In the present invention, an aerated fermentation tank is filled with alcohol, water, acetic acid fermentation liquid or acetic acid, and a moromi prepared using nutrients for acetic acid bacteria, inoculated with acetic acid bacteria that have been acclimated to an acetic acid concentration of 15% or more, and then fermented under aeration. Fermentation is started, and when the fermentation progresses and the acetic acid concentration in the moromi rises to a sufficient level and the alcohol concentration reaches 0.7 to 2%, without interrupting aeration, leave part of the moromi and take out the rest, and then remove the raw moromi. In the semi-continuous fermentation method, which repeats the cycle by refilling the moromi to continue fermentation, then taking out a portion of the moromi in the same manner, and then refilling the raw moromi, the acetic acid concentration of the moromi increases. The temperature of the moromi is set at 27-32℃ until it reaches 12-15%, and then the temperature of the moromi is lowered to below 27℃ with 18℃ as the lower limit, and the target acetic acid concentration and alcohol concentration are 20% or more. When the concentration reaches 0.7 to 2%, leave some of the moromi and take out the rest without interrupting the aeration, then refill the raw moromi and continue fermentation in the same way as the previous cycle, and repeat the same cycle again. This method of producing vinegar is characterized by obtaining an acetic acid fermentation liquid having a high acetic acid concentration of 20% or more by performing semi-continuous fermentation using an aerated fermentation method by repeating the steps. The present invention will be explained in detail below. Conventionally, when producing vinegar using the aerated fermentation method, although the methods vary, the fermentation temperature range is 26-40℃ throughout the fermentation period, usually 28℃.
Temperatures of ~32°C have been employed. This temperature condition has been set as the optimum temperature for the production of vinegar by the aerated fermentation method, and has also been considered important in order to minimize changes in the environment for acetic acid bacteria. However, the present inventors discovered that in acetic acid fermentation under aeration, the acetic acid bacteria used have two periods during which they grow together with the bioacid (hereinafter referred to as the "growth phase") and a period during which they stop growing and continue to produce only the bioacid (hereinafter referred to as "the growth phase"). We believe that keeping the temperature the same throughout these two periods is the main reason why it has been difficult to reach high acetic acid concentrations in the past. That is, as a result of various studies focusing on the characteristics of this acetic acid bacterium, the present inventors first discovered that the optimum temperature is different during the growth phase and the bioacidic phase, and based on this, the optimum temperature is different during the growth phase. , a vinegar manufacturing method in which the temperature of the moromi is set at 27 to 32°C, which is conventionally known, and then the temperature of the moromi is lower than the temperature during the growth stage, that is, 18 to 24°C (patent application 1973). -14216 (Special Publication No. 56-21389)), production of vinegar that lowers the temperature of the moromi within a range not exceeding 2°C as the acetic acid concentration increases when lowering the temperature of the moromi during the bioacid period. Law (Special application 1977-129891)
(Japanese Unexamined Patent Publication No. 56-55193)), and a method for producing vinegar that combines aerated fermentation in which the temperature of the moromi is lowered during the acid stage and a semi-continuous fermentation method using aerated fermentation (Japanese Patent Application No. 54-136373). (Japanese Unexamined Patent Publication No. 56-61987)). After that, we continued various studies on the acetic acid bacteria used for fermentation, the alcohol concentration at the time of taking out the moromi in the semi-continuous fermentation cycle, and the temperature setting of the moromi, and finally achieved over 20% in the semi-continuous fermentation method using aerated fermentation. The present invention has been achieved, which makes it possible to obtain an acetic acid fermentation solution having a high acetic acid concentration. First, the results of a study on acetic acid bacteria used for fermentation will be explained using experimental examples. Experimental Example 1 Refilling the aerated fermentation tank with alcohol, water, acetic acid fermentation liquid, and moromi prepared using acetic acid bacteria nutrients,
When the temperature inside the tank reached 30°C, acetic acid bacteria were inoculated and fermentation was started under ventilation, and the temperature of the moromi was then controlled at approximately 30°C using a temperature controller. At that time, the acetic acid concentration was 6.5% and the alcohol concentration was 3.5%. When fermentation progressed and the acetic acid concentration reached 8.8%, addition of alcohol with an alcohol concentration of approximately 50% was started. Fermentation progresses further and the acetic acid concentration is approximately 13
%, change the setting of the temperature controller and set it to 26℃.
After that, the acetic acid concentration will be about 15%, about 17%, and about 19%.
Set the temperature controller to 24℃, 22℃, and 20℃ respectively.
When the acetic acid concentration reached 20.5%, part of the moromi was left behind and the rest was taken out, the raw moromi was refilled, and the next cycle of fermentation was started, and the fermentation was continued in the same way as the previous cycle. In this case, acetic acid bacteria in a fermenter carrying out the following fermentation were used as the acetic acid bacteria, and the effect of this on fermentation was investigated. The results are shown in Table 1. Category A: Continuous fermentation is carried out at an acetic acid concentration of 6%.Acetic acid bacteria category B: Semi-continuous fermentation is carried out at an acetic acid concentration of 12-13%.Acetic acid bacteria category C: Semi-continuous fermentation is carried out at an acetic acid concentration of 15-16%. Category D of acetic acid bacteria: Acetic acid bacteria that perform semi-continuous fermentation at an acetic acid concentration of 12 to 13%, and occasionally perform a cycle of removing the mash at a concentration of 15 to 16%.

【表】 上記実験の結果から、生酸期の醪の温度を低温
にすることにより通気下の酢酸発酵が可能な酢酸
菌であれば、通気発酵により酢酸濃度20%以上ま
で発酵はできるものの、原料醪再充填後に再び酢
酸濃度20%以上まで発酵できること、すなわち半
連続発酵のサイクルが継続できることは、少なく
とも酢酸濃度15%以上で馴養された酢酸菌を用い
ることにより初めて可能であることがわかつた。 上記の如く本発明においては、用いる酢酸菌の
選択が重要であるが、一般に通気発酵法による半
連続発酵を行なうにあたつては、取り出される醪
のアルコール濃度が0に近い状態になれば、酢酸
菌に決定な損傷を与え、発酵が停止してしまうこ
とが知られており、また一方、アルコールを多く
残して醪を取り出すことは経済的にデメリツトで
あることなどから、その濃度は概ね0.3〜0.5%が
適当とされている。 しかしながら、本発明者等は、次の様な実験を
行なつて酢酸濃度20%以上を有する酢酸発酵液を
得ることのできる通気発酵法による半連続発酵を
効率良く行なうための醪取り出し時の醪のアルコ
ール濃度について検討した。 実験例 2 実験例1で用いたと同様の通気発酵槽に、アル
コール、水、酢酸発酵液、及び酢酸菌の栄養物を
用いて調製した醪を充填し、これに酢酸濃度15%
台で半連続発酵を行なつている酢酸菌を接種して
通気下に発酵を開始し、実験例1と同様にしてア
ルコールの添加と醪の温度の調節を行ないつつ、
酢酸濃度が20%以上になつたところで通気を中断
することなく醪の一部を残して他は取り出し、原
料醪を再充填し、前のサイクルと同様にして発酵
を継続させた。 この醪を取り出す時のアルコール濃度を種々変
えてこれが発酵に及ぼす影響を調べた。その結果
を示すと第2表のとおりである。
[Table] From the results of the above experiments, it was found that if the acetic acid bacteria are capable of acetic acid fermentation under aeration by lowering the temperature of the moromi during the raw acid stage, they can ferment to an acetic acid concentration of 20% or more through aeration fermentation. It was found that being able to ferment again to an acetic acid concentration of 20% or more after refilling the raw mash, that is, being able to continue a semi-continuous fermentation cycle, is only possible by using acetic acid bacteria that have been acclimated to at least an acetic acid concentration of 15% or more. . As mentioned above, in the present invention, the selection of the acetic acid bacteria used is important, but in general, when performing semi-continuous fermentation using the aerated fermentation method, if the alcohol concentration of the moromi to be taken out is close to 0, It is known that it causes severe damage to acetic acid bacteria and stops fermentation, and on the other hand, it is economically disadvantageous to remove the moromi with a large amount of alcohol left behind, so the concentration is approximately 0.3. ~0.5% is considered appropriate. However, the present inventors conducted the following experiments and determined how to improve the quality of the moromi at the time of taking out the moromi in order to efficiently carry out semi-continuous fermentation using the aerated fermentation method, which can obtain an acetic acid fermentation liquid having an acetic acid concentration of 20% or more. We investigated the alcohol concentration of Experimental Example 2 An aerated fermentation tank similar to that used in Experimental Example 1 was filled with moromi prepared using alcohol, water, acetic acid fermentation liquid, and nutrients for acetic acid bacteria, and the acetic acid concentration was 15%.
We inoculated acetic acid bacteria that were undergoing semi-continuous fermentation on a stand, and started fermentation under ventilation.While adding alcohol and adjusting the temperature of the moromi in the same manner as in Experimental Example 1,
When the acetic acid concentration reached 20% or more, without interrupting aeration, part of the moromi was left and the rest was taken out, the raw moromi was refilled, and fermentation was continued in the same way as in the previous cycle. The alcohol concentration at the time of taking out the moromi was varied and the effect of this on fermentation was investigated. The results are shown in Table 2.

【表】【table】

【表】 上記の実験の結果から、0.7%より小なるアル
コール濃度、すなわち従来より公知の0.5%以下
のアルコール濃度の時に醪の取り出しと原料醪の
再充填を行なうことは、半連続発酵の継続は可能
であるが、平均生酸速度が低く、言い換えれば発
酵に長時間要することとなり、効率的に悪いこと
がわかつた。一方、醪の取り出し時のアルコール
濃度が2%以上では、添加するアルコールの量が
他に較べて多くなるために発酵に影響を与えるこ
となどからメリツトがない。従つて酢酸濃度20%
以上を有する酢酸発酵液を得ることのできる通気
発酵法による半連続発酵を行なうにあたつては、
醪の取り出し時のアルコール濃度を0.7〜2%と
することが適当であることがわかつた。 つぎに本発明の半連続発酵においても、酢酸濃
度20%以上を有する酢酸発酵液を得るためには、
増殖期(すなわち醪中の酢酸濃度が12〜15%とな
るまで)においては醪の温度を27〜32℃とする
が、酢酸濃度12〜15%に達した以後は18℃を下限
として醪の温度を27℃より低い温度に下げていく
ことが重要である。この点について実験例を挙げ
て説明する。 実験例 3 実験例1で用いたと同様の通気発酵槽にアルコ
ール、水、酢酸発酵液、及び酢酸菌の栄養物を用
いて調製した醪を充填し、槽内の温度が30℃とな
つたところで、酢酸濃度15%台で半連続発酵を行
なつている酢酸菌を接種して通気下に発酵を開始
し、その後温調計により醪の温度を約30℃に制御
した。その時の酢酸濃度は6.8%であり、アルコ
ール濃度は3.2%であつた。 そして発酵が進行して酢酸濃度が8.5%となつ
たところでアルコール濃度が約50%のアルコール
の添加を開始し、酢酸濃度が増加してきたところ
で醪の温度を制御する温調計の設定を変更するこ
とにより醪の温度を26℃に下げた。この時、温度
を下げ始める時の酢酸濃度を種々変え、その酢酸
濃度に達する前4時間及び達した後4時間の平均
生酸速度について検討した。その結果を第3表に
示す。 なお、第3表中の平均生酸速度AおよびBは次
式より算出したものである。 A=X−Y/4 B=Z−X/4 X:温度を変更した時の酢酸濃度(%) Y:温度を変更する4時間前の酢酸濃度(%) Z:温度を変更して4時間後の酢酸濃度(%)
[Table] From the results of the above experiments, it was found that removing the moromi and refilling the raw moromi at an alcohol concentration of less than 0.7%, that is, the conventionally known alcohol concentration of 0.5% or less, is the best way to continue semi-continuous fermentation. Although it is possible, it was found that the average bioacid rate is low, in other words, it takes a long time for fermentation, and it is inefficient. On the other hand, if the alcohol concentration at the time of taking out the moromi is 2% or more, there is no advantage because the amount of alcohol added will be larger than others, which will affect fermentation. Therefore, the acetic acid concentration is 20%
In carrying out semi-continuous fermentation using the aerated fermentation method that can obtain an acetic acid fermentation liquid having the above,
It was found that it is appropriate to set the alcohol concentration at the time of taking out the moromi from 0.7 to 2%. Next, in the semi-continuous fermentation of the present invention, in order to obtain an acetic acid fermentation liquid having an acetic acid concentration of 20% or more,
During the growth phase (that is, until the acetic acid concentration in the moromi reaches 12-15%), the temperature of the moromi is kept at 27-32℃, but after the acetic acid concentration reaches 12-15%, the lower limit is 18℃. It is important to reduce the temperature to below 27°C. This point will be explained using an experimental example. Experimental Example 3 An aerated fermentation tank similar to that used in Experimental Example 1 was filled with moromi prepared using alcohol, water, acetic acid fermentation liquid, and nutrients for acetic acid bacteria, and when the temperature inside the tank reached 30°C. After inoculating the acetic acid bacteria that were performing semi-continuous fermentation at an acetic acid concentration of 15%, fermentation was started under aeration, and the temperature of the moromi was then controlled at approximately 30°C using a temperature controller. At that time, the acetic acid concentration was 6.8% and the alcohol concentration was 3.2%. When the fermentation progresses and the acetic acid concentration reaches 8.5%, the addition of alcohol with an alcohol concentration of approximately 50% is started, and as the acetic acid concentration increases, the settings of the temperature controller that controls the temperature of the moromi are changed. As a result, the temperature of the moromi was lowered to 26℃. At this time, the acetic acid concentration at the time when the temperature started to be lowered was varied, and the average bioacid rate for 4 hours before reaching the acetic acid concentration and 4 hours after reaching the acetic acid concentration was investigated. The results are shown in Table 3. Note that the average bioacid rates A and B in Table 3 were calculated using the following formula. A=X-Y/4 B=Z-X/4 Acetic acid concentration after time (%)

【表】 この実験結果から、醪の酢酸濃度が12〜15%の
時、好ましくは12〜13%の時に温度を低下させ始
めると生酸速度にほとんど影響を与えないことが
わかり、従つて温度を低下し始める時の酢酸濃度
は12〜15%、好ましくは12〜13%が適当であるこ
とがわかる。 更に次の実験を行なうことにより、醪の最終設
定温度即ち醪の取り出し時の温度について検討し
た。 実験例 4 実験例1で用いたと同様の通気発酵槽にアルコ
ール、水、酢酸発酵液及び酢酸菌の栄養物を用い
て調製した醪を充填し、槽内の温度が30℃となつ
たところで、酢酸濃度15%台で半連続発酵を行な
つている酢酸菌を接種して通気下に発酵を開始
し、その後温調計により醪の温度を約30℃に制御
した。その時の酢酸濃度は6.8%、アルコール濃
度は3.6%であつた。 そして発酵が進み、酢酸濃度が8.5%となつた
ところで、実験例1に記載したと同様のアルコー
ルの添加を開始した。さらに発酵が進み、酢酸濃
度が約13%となつたところで、温調計の設定を変
更して26℃とし、以後酢酸濃度が約15%、約17
%、約19%の時、温調計の設定を変更して醪の温
度を低下させ、酢酸濃度が20%以上となつたとこ
ろで、通気を中断することなく醪の一部を残して
他は取り出し、原料醪を再充填して次のサイクル
の発酵を開始し、前のサイクルと同様にして発酵
を継続させた。 以下同様にしてサイクルを繰り返すうち、酢酸
濃度が約19%の時に設定した温度、すなわち醪の
取り出し時の温度を種々変えて次のサイクルへの
影響を調べた結果を第4表に示す。
[Table] From the results of this experiment, it is clear that if the temperature starts to decrease when the acetic acid concentration in the moromi is 12 to 15%, preferably 12 to 13%, it has little effect on the rate of bioacid; It can be seen that the appropriate acetic acid concentration is 12 to 15%, preferably 12 to 13%, when the concentration of acetic acid begins to decrease. Furthermore, by conducting the following experiment, we investigated the final set temperature of the moromi, that is, the temperature at the time of taking out the moromi. Experimental Example 4 An aerated fermentation tank similar to that used in Experimental Example 1 was filled with moromi prepared using alcohol, water, acetic acid fermentation liquid, and nutrients for acetic acid bacteria, and when the temperature inside the tank reached 30°C, Acetic acid bacteria, which are performing semi-continuous fermentation at an acetic acid concentration of 15%, were inoculated and fermentation was started under aeration, after which the temperature of the moromi was controlled at approximately 30°C using a temperature controller. At that time, the acetic acid concentration was 6.8% and the alcohol concentration was 3.6%. When the fermentation progressed and the acetic acid concentration reached 8.5%, addition of alcohol as described in Experimental Example 1 was started. When the fermentation progressed further and the acetic acid concentration reached approximately 13%, the temperature controller was changed to 26℃, and from then on the acetic acid concentration increased to approximately 15% and approximately 17%.
%, about 19%, change the setting of the temperature controller to lower the temperature of the moromi, and when the acetic acid concentration reaches 20% or more, leave some of the moromi without interrupting the aeration and remove the rest. The fermentation was then carried out in the same manner as in the previous cycle, and the next cycle of fermentation was continued. While repeating the cycle in the same manner, the temperature set when the acetic acid concentration was about 19%, that is, the temperature at the time of taking out the moromi, was varied, and the influence on the next cycle was investigated. The results are shown in Table 4.

【表】 この実験結果から、最終温度を18℃以下にする
と、次のサイクルの初期に誘導期を生じ、酢酸濃
度が20℃以上に達するものの平均生酸速度が低
く、言い換えれば発酵時間が長くなつて効率が悪
くなることから、醪の温度の下限としては18℃と
するのが適当であることがわかる。 本発明では、上記の如く酢酸濃度15%以上で馴
養した酢酸菌を用いて通気下に発酵を開始し、醪
の酢酸濃度が12〜15%となるまでは醪の温度を27
〜32℃とし、その後醪の温度を18℃を下限として
27℃より低い温度に低下させて酢酸濃度20%以
上、アルコール濃度0.7〜2%となつたところで
醪の取り出しと原料醪の再充填を行なつて同様に
発酵を継続させることにより半連続発酵を行なう
こと以外は、従来の通気発酵法による食酢の製造
に従つて実施することができる。 すなわち醪としては、アルコール、水、酢酸発
酵液または酢酸、及び酢酸菌の栄養物(例えば酒
粕浸出液、酵母エキス、無機塩類、糖類、有機酸
のうち適当なもの)で調製した醪が用いられる。
発酵を行なう通気発酵タンクとしては主原料であ
るアルコール、主生産物である酢酸が共に揮発性
であるため、比較的少量の通気(例えば毎分醪量
に対して5〜30%)が十分混合されるようなタン
ク(例えば通気攪拌式発酵装置、エアーリフト型
発酵装置、気体巻き込み式培養装置など)が用い
られる。さらに酢酸菌の接種の方法や発酵終了後
の酢酸発酵液を食酢にするための熟成、過、殺
菌なども常法にしたがつて行なうことができる。 かくして本発明によれば、通気発酵法による半
連続発酵で20%以上の高い酢酸濃度を有する酢酸
発酵液を効率よく得ることができ、この酢酸発酵
液を常法により熟成、過、及び殺菌して20%以
上の高い酢酸濃度の食酢を製造することができ
る。しかも、本発明では、半連続発酵が行なえる
ことから、発酵槽は1台で済み、増殖槽と生酸槽
に分けたりする必要がなく、効率よく発酵を行な
うことができるので、本発明は通気発酵による食
酢の製造法として非常に有用な方法である。 次に本発明の実施例を示す。 実施例 外部から導入した空気を微粉砕してタンク内の
液に分散させるための攪拌翼、温調用コイル、及
び消泡機を備え、空気の流量計を接続した全容量
25000の通気発酵タンクに、変性アルコール、
水、未過のホワイトビネガー、糖、無機塩類、
酵母エキス等の栄養物を混合して調製した酢酸濃
度6.8%、アルコール濃度3.2%の醪14000を仕
込み毎分約2000の通気量で通気攪拌を開始
し、醪の温度が30℃となつたところで温調計を作
動させ29.8〜30.2℃に醪の温度を保持した。 一方、全容量20000の上記と同様な通気発酵
タンクに、上記と同様の原料からなる醪を仕込
み、酢酸濃度15%台で半連続発酵を行なつている
うち、原料醪の再充填が完了した後、酢酸濃度が
約7%となつたところで、この醪2000を通気を
中断することなく、自給式ポンプで急速に前記
25000の通気発酵タンクの醪に接種した。この
時、接種した醪のアルコール濃度は約3.5%であ
つた。そして接種された通気発酵タンクの醪の酢
酸濃度は6.82%、アルコール濃度は3.68%であつ
た。 接種後5時間で、酢酸濃度は0.54%上り、誘導
期が短かく発酵が開始したのを認めた。さらに7
時間後に酢酸濃度が8.5%となり、アルコール濃
度が1.9%となつたところで、約50%のアルコー
ル濃度を有する変性アルコールの添加を開始し
た。 アルコールの添加を開始してから18時間後に酢
酸濃度が12.8%となつたので、温調計の設定を26
℃とした。その後、12時間目、25時間目、40時間
目に温調計の設定をそれぞれ24℃、22℃、20℃と
したが、その後の酢酸濃度はそれぞれ15.3%、
17.2%、19.3%であつた。更に50時間目には酢酸
濃度20.5%、アルコール濃度2.0%となつたの
で、アルコールの添加を中止したが、この時点で
醪の全容量は約23000となつた。 更に発酵を継続し、温調計の設定を変更し始め
てから59時間目に酢酸濃度21.5%、アルコール濃
度1%となつたので、醪約18500を通気を中断
することなく取り出し、新たに変性アルコール、
水、未過のホワイトネガー、糖、無機塩類、酵
母エキス等の栄養物よりなり酢酸濃度1%、アル
コール濃度5%の原料醪約11500の充填を開始
すると同時に温調計の設定を変更して30℃とし
た。 原料醪再充填後の酢酸濃度は6.77%、アルコー
ル濃度は3.88%であつた。原料醪再充填後13時間
目には酢酸濃度が8.6%、アルコール濃度2%と
なつたので、前のサイクルと同様の変性アルコー
ルの添加を開始した。その後は前のサイクルと同
様にして酢酸濃度が13.2%、15.4%、18.0%、
19.1%の時、それぞれ26℃、24℃、22℃、20℃に
温調計の設定を変更した。変性アルコールの添加
を開始してから68時間目に酢酸濃度が20.6%、ア
ルコール濃度1.9%となつたので、変性アルコー
ルの添加を中止したが、この時点で醪の全容量は
約23000となつた。 更に発酵を継続し、変性アルコールの添加を開
始してから77時間目に酢酸濃度21.6%、アルコー
ル濃度0.9%となつたので、前回と同様にして醪
の取り出しと、原料醪の再充填、及び温調計の設
定変更を行ない、以下上記したと同様の操作を行
なつて発酵を継続した。 このようなサイクルを繰り返すことにより、半
連続発酵法で20%以上の高い酢酸濃度を有する酢
酸発酵液を得、これを熟成、過、殺菌して高い
酢酸濃度の食酢を得た。
[Table] From the results of this experiment, when the final temperature is lower than 18℃, an induction period occurs at the beginning of the next cycle, and although the acetic acid concentration reaches 20℃ or higher, the average bioacid rate is low, in other words, the fermentation time is longer. Since the efficiency deteriorates as the temperature ages, it is clear that a lower limit of the temperature of the moromi is 18°C. In the present invention, fermentation is started under aeration using acetic acid bacteria that have been acclimated to an acetic acid concentration of 15% or more as described above, and the temperature of the moromi is kept at 27°C until the acetic acid concentration of the moromi reaches 12 to 15%.
~32℃, then lower the temperature of the moromi to 18℃.
Semi-continuous fermentation is carried out by lowering the temperature to below 27°C, and when the acetic acid concentration reaches 20% or more and the alcohol concentration reaches 0.7 to 2%, the moromi is taken out and the raw moromi is refilled, and fermentation is continued in the same way. Other than the above, it can be carried out in accordance with the conventional production of vinegar by the aerated fermentation method. That is, as the moromi, a moromi prepared with alcohol, water, acetic acid fermentation liquid or acetic acid, and nutrients for acetic acid bacteria (for example, a suitable one among sake lees infusion, yeast extract, inorganic salts, sugars, and organic acids) is used.
In the aerated fermentation tank where fermentation takes place, alcohol, the main raw material, and acetic acid, the main product, are both volatile, so a relatively small amount of aeration (for example, 5 to 30% of the mash content per minute) is necessary to ensure sufficient mixing. A tank (for example, an aerated stirring type fermenter, an air lift type fermenter, a gas entrainment type culture apparatus, etc.) is used. Furthermore, inoculation of acetic acid bacteria and aging, filtration, and sterilization of the acetic acid fermentation liquid to make vinegar after completion of fermentation can be carried out according to conventional methods. Thus, according to the present invention, it is possible to efficiently obtain an acetic acid fermentation liquid having a high acetic acid concentration of 20% or more by semi-continuous fermentation using the aerated fermentation method, and this acetic acid fermentation liquid is aged, filtered, and sterilized by conventional methods. It is possible to produce vinegar with a high acetic acid concentration of 20% or more. Moreover, in the present invention, since semi-continuous fermentation can be performed, only one fermenter is required, and there is no need to separate it into a growth tank and a raw acid tank, and fermentation can be carried out efficiently. This is a very useful method for producing vinegar by aerated fermentation. Next, examples of the present invention will be shown. Example: A full-capacity unit equipped with a stirring blade, temperature control coil, and defoamer to finely pulverize air introduced from the outside and disperse it into the liquid in the tank, and connected to an air flow meter.
Denatured alcohol in a 25000 aerated fermentation tank,
Water, unfiltered white vinegar, sugar, inorganic salts,
A 14,000 mash with an acetic acid concentration of 6.8% and an alcohol concentration of 3.2% prepared by mixing nutrients such as yeast extract was prepared, and aeration stirring was started at an aeration rate of approximately 2,000 m/min. When the temperature of the moromi reached 30℃. The temperature controller was operated to maintain the temperature of the moromi at 29.8-30.2°C. Meanwhile, a fermentation tank similar to the one above with a total capacity of 20,000 liters was charged with moromi made from the same raw materials as above, and while semi-continuous fermentation was being carried out at an acetic acid concentration of 15%, refilling of the raw material moromi was completed. After that, when the acetic acid concentration reached about 7%, this moromi 2000 was rapidly pumped to the above level using a self-contained pump without interrupting the aeration.
The moromi in a 25,000 aerated fermentation tank was inoculated. At this time, the alcohol concentration of the inoculated moromi was approximately 3.5%. The acetic acid concentration and alcohol concentration of the moromi in the inoculated aerated fermentation tank were 6.82% and 3.68%, respectively. Five hours after inoculation, the acetic acid concentration increased by 0.54%, indicating that the induction period was short and fermentation had started. 7 more
After a period of time, when the acetic acid concentration reached 8.5% and the alcohol concentration reached 1.9%, addition of denatured alcohol having an alcohol concentration of about 50% was started. 18 hours after starting the addition of alcohol, the acetic acid concentration reached 12.8%, so the temperature controller was set to 26.
℃. After that, the temperature controller was set to 24℃, 22℃, and 20℃ at the 12th, 25th, and 40th hours, respectively, and the acetic acid concentration after that was 15.3% and 20℃, respectively.
They were 17.2% and 19.3%. Furthermore, at the 50th hour, the acetic acid concentration was 20.5% and the alcohol concentration was 2.0%, so the addition of alcohol was stopped, but at this point the total volume of the moromi was about 23,000. Further fermentation continued, and at 59 hours after starting to change the temperature controller settings, the acetic acid concentration was 21.5% and the alcohol concentration was 1%. Therefore, approximately 18,500 mash was taken out without interrupting the aeration, and newly denatured alcohol was added. ,
At the same time as we started filling approximately 11,500 ml of raw material moromi with an acetic acid concentration of 1% and an alcohol concentration of 5%, consisting of nutrients such as water, unfiltered white negative, sugar, inorganic salts, and yeast extract, we changed the settings of the temperature controller. The temperature was set at 30℃. After refilling the raw mash, the acetic acid concentration was 6.77% and the alcohol concentration was 3.88%. Thirteen hours after refilling the raw mash, the acetic acid concentration was 8.6% and the alcohol concentration was 2%, so addition of denatured alcohol was started in the same way as in the previous cycle. After that, as in the previous cycle, the acetic acid concentration was 13.2%, 15.4%, 18.0%,
At 19.1%, the temperature controller settings were changed to 26°C, 24°C, 22°C, and 20°C, respectively. 68 hours after starting the addition of denatured alcohol, the acetic acid concentration was 20.6% and the alcohol concentration was 1.9%, so the addition of denatured alcohol was stopped, but at this point the total volume of the moromi was approximately 23,000. . Fermentation continued, and 77 hours after starting the addition of denatured alcohol, the acetic acid concentration was 21.6% and the alcohol concentration was 0.9%, so we removed the moromi, refilled the raw moromi, and The settings of the temperature controller were changed, and the same operations as described above were performed to continue fermentation. By repeating such a cycle, an acetic acid fermentation liquid having a high acetic acid concentration of 20% or more was obtained by a semi-continuous fermentation method, and this was aged, filtered and sterilized to obtain vinegar with a high acetic acid concentration.

Claims (1)

【特許請求の範囲】[Claims] 1 通気発酵タンクにアルコール、水、酢酸発酵
液または酢酸、及び酢酸菌の栄養物を用いて調製
した醪を充填し、酢酸濃度15%以上で馴養した酢
酸菌を接種して通気下に発酵を開始させ、その後
発酵が進行し醪の酢酸濃度が充分上りアルコール
濃度が0.7〜2%となつたところで通気を中断す
ることなく醪の一部を残して他は取り出し、次に
原料醪を再充填して発酵を継続させ、以下同様に
して醪の一部を取り出し、次に原料醪を再充填す
るというようにしてサイクルを繰り返す半連続発
酵法での連続するサイクルにおいて、醪の酢酸濃
度が12〜15%となるまでは醪の温度を27〜32℃と
し、その後18℃を下限として醪の温度を27℃より
低い温度に低下させ20%以上の目的とする酢酸濃
度及びアルコール濃度が0.7〜2%となつたとこ
ろで通気を中断することなく醪の一部を残して他
は取り出し、次に原料醪を再充填して前回のサイ
クルと同様にして発酵を継続させ、さらに同様の
サイクルを繰り返すことによる通気発酵法で半連
続発酵を行なうことにより、20%以上の高い酢酸
濃度を有する酢酸発酵液を得ることを特徴とする
食酢の製造法。
1 Fill an aerated fermentation tank with alcohol, water, acetic acid fermentation liquid or acetic acid, and a moromi prepared using nutrients for acetic acid bacteria, inoculate with acetic acid bacteria that have been acclimated to an acetic acid concentration of 15% or more, and ferment under aeration. After fermentation has progressed and the acetic acid concentration in the moromi has increased sufficiently and the alcohol concentration has reached 0.7 to 2%, without interrupting the aeration, leave part of the moromi and take out the rest, and then refill the raw moromi. In successive cycles of the semi-continuous fermentation method, in which a part of the moromi is taken out in the same manner and then refilled with the raw moromi, the cycle is repeated, the acetic acid concentration of the moromi reaches 12 The temperature of the moromi is set at 27 to 32℃ until it reaches ~15%, and then the temperature of the moromi is lowered to below 27℃ with 18℃ as the lower limit, and the target acetic acid concentration and alcohol concentration are 0.7 to 20%. When it reaches 2%, leave some of the moromi and take out the rest without interrupting the aeration, then refill the raw moromi and continue fermentation in the same way as the previous cycle, and repeat the same cycle. A method for producing table vinegar, characterized in that an acetic acid fermentation liquid having a high acetic acid concentration of 20% or more is obtained by performing semi-continuous fermentation using an aerated fermentation method.
JP11029480A 1980-08-13 1980-08-13 Production of vinegar Granted JPS5736976A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP11029480A JPS5736976A (en) 1980-08-13 1980-08-13 Production of vinegar

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP11029480A JPS5736976A (en) 1980-08-13 1980-08-13 Production of vinegar

Publications (2)

Publication Number Publication Date
JPS5736976A JPS5736976A (en) 1982-02-27
JPS6236669B2 true JPS6236669B2 (en) 1987-08-07

Family

ID=14532042

Family Applications (1)

Application Number Title Priority Date Filing Date
JP11029480A Granted JPS5736976A (en) 1980-08-13 1980-08-13 Production of vinegar

Country Status (1)

Country Link
JP (1) JPS5736976A (en)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS60207579A (en) * 1984-03-30 1985-10-19 Nakano Vinegar Co Ltd Preparation of vinegar
JPH035793Y2 (en) * 1985-03-06 1991-02-14

Also Published As

Publication number Publication date
JPS5736976A (en) 1982-02-27

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